510(k) K151576 ยท GXY Electrode, Cutaneous
Neon EEG
| Applicant | Incereb, Ltd., Dublin, IE |
| Decision | Substantially Equivalent, Sep 29, 2015 |
| Received | Jun 11, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151576
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.